A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525652



Internal ID15106259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:119486243..119565357hg38UCSC Ensembl
InnerchrX:118620206..118699320hg19UCSC Ensembl
InnerchrX:118504234..118583348hg18UCSC Ensembl
InnerchrX:118402088..118481202hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3879115
hg1979115
hg1879115
hg1779115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701807
Samples
Known GenesCXorf56
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525652
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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